Canonical Allele Identifier: PA2830302973
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 373720
ClinVar RCV Id: RCV000413936 RCV000945894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689601.2:p.Arg25Cys
CA2056583
NM_152388.4:c.73C>T